AU705240B2 - Composition suitable for inhibiting potato sprouting and/or fungoid growth - Google Patents

Composition suitable for inhibiting potato sprouting and/or fungoid growth Download PDF

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AU705240B2
AU705240B2 AU61900/98A AU6190098A AU705240B2 AU 705240 B2 AU705240 B2 AU 705240B2 AU 61900/98 A AU61900/98 A AU 61900/98A AU 6190098 A AU6190098 A AU 6190098A AU 705240 B2 AU705240 B2 AU 705240B2
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carvone
composition
potatoes
sprouting
inhibiting
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Pieter Diepenhorst
Klaasje Jannie Hartmans
Franciscus Van Kleef
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Adama Agriculture BV Amsterdam NL Schaffhausen Branch
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Chemische Pharmaceutische Industrie "Luxan" BV
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23BPRESERVING, e.g. BY CANNING, MEAT, FISH, EGGS, FRUIT, VEGETABLES, EDIBLE SEEDS; CHEMICAL RIPENING OF FRUIT OR VEGETABLES; THE PRESERVED, RIPENED, OR CANNED PRODUCTS
    • A23B7/00Preservation or chemical ripening of fruit or vegetables
    • A23B7/14Preserving or ripening with chemicals not covered by groups A23B7/08 or A23B7/10
    • A23B7/153Preserving or ripening with chemicals not covered by groups A23B7/08 or A23B7/10 in the form of liquids or solids
    • A23B7/154Organic compounds; Microorganisms; Enzymes
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N31/00Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/06Oxygen or sulfur directly attached to a cycloaliphatic ring system
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N31/00Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/08Oxygen or sulfur directly attached to an aromatic ring system
    • A01N31/14Ethers
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N35/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
    • A01N35/06Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals

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  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Agronomy & Crop Science (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Environmental Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Chemical & Material Sciences (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Preparation Of Fruits And Vegetables (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pretreatment Of Seeds And Plants (AREA)
  • Cultivation Of Plants (AREA)

Abstract

PCT No. PCT/NL94/00240 Sec. 371 Date Sep. 20, 1996 Sec. 102(e) Date Sep. 20, 1996 PCT Filed Oct. 3, 1994 PCT Pub. No. WO95/09536 PCT Pub. Date Apr. 13, 1995A composition suitable for inhibiting potato sprouting and inhibiting the growth of fungi and decay bacteria, including a mixture of carvone and menthol, a method for inhibiting potato sprouting by using such composition and the use thereof, and a composition in the form of an emulsion or granulate which includes carvone and menthol or carvone alone, giving rise to a delayed release of the active compound and an extension of the length of sprout inhibition.

Description

AUSTRALIA
PATE NTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANT(S): B.V. Clieniische Piarnceutische Industric "Luxan" ADDRE SS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street Melbourne, 3000.
INVENTION TITLE: Composition suitable for iiihibiting potato sprouting and/or fungoidI growth The -following statemnent, is a full description of* this invention, including thle best method of' performing it known to us: r oPER Pj1[11! j~1Y'v 1' 1U1.4IR o 0.0.00 0* 0 0 *0 0 0 000 0 0 Title: Composition suitable for inhibiting potato sprouting and/or fungoid growth.
This invention relates to a composition which is suitable for inhibiting potato sprouting and/or fungoid growth, and to the use of that composition in controlling patato sprouting and/or fungoid growth in potatoes.
Potato sprouting, also referred to as shooting, poses a problem in the storage of potatoes. In fact, sprouting leads to potato quality loss because it results in loss of weight, the turgor of the potatoes lessens (the potatoes become softer) and toxic products may be formed in the sprouts.
Sprouting can be inhibited by storing the potatoes at a temperature of 2 0 C, but at such a low temperature reducing sugars are formed which give a brown color to the potatoes when (deep)fried and cause them to taste sweet. For this reason the potatoes are typically stored at a temperature between 5 and 8°C. At such a temperature the problem of the formation of reducing sugars is absent or considerably smaller, but sprouting upon prolonged storage is not entirely avoided.
Therefore, sprouting inhibitors are necessary to maintain potato quality during storage, both in potatoes intended fcr direct consumption and in potatoes to be processed into po ato products. Such sprouting inhibitors are used to inhibit sprouting over prolonged storage periods at lower temperatares, i.e. below 100C, Chemical sprouting inhibitors have been utilized with success for over two decades to prevent sprouting or shooting during the storage of potatoes. Propham (IPC) and chlorpropham S(CIPC), which were originally developed as herbicides, are utilized as sprout inhibitors on a large scale in Europe, 30 while in America maleic acid anhydride is used as well. In SEngland, tecnazene is still being used as a sprout inhibitor.
These last two inhibitors are probably going to be forbidden in the near future. Nor is the future of IPC and CIPC certain, since there is a tendency to lower the maximum 35 residue level (MRL) of such compocnds on potatoes. Also, the market for untreated potatoes potatoes not treated with chemicals) is rapidly expanding.
i 1 Accordingly, there is a need for alternatives to these sprout inhibitors.
Replacement sprout inbibitors must satisfy the following requirements: they must preferably be effective at a low dose and easy to use; they must preferably be of vegetable origin, non-toxic, colorless, tasteless and odorless; they must not affect the properties of the potatoes or their processability; and they must be acceptable in connection with the regulations applicable to such products.
Products which satisfy these requirements have been known to date. A number of monoterpenes from plants show interesting possibilities as alternative sprout inhibitors. One of these compounds is carvone, which compound is present in the essential oil of the seeds of the caraway plant (Carum carvi).
This compound is also of interest because it is registered as a food additive and has the so-called "GRAS" status (Generally Recognized As Safe). Moreover, it is possible to grow caraway on a commercial scale. This is already happening on a large scale in various countries both inside and outside Europe.
Caraway seed contains approximately 3 to 5% essential oil.
Approximately one-half thereof consists of D-carvone, the other half is D-limonene, in addition to a few percent of other isoprenoids. D-limonene does not have sufficient influence on sprouting and can be removed through fractionated distillation, so that a D-carvone enriched (90-95%) caraway oil is obtained.
S. 30 D-carvone further occurs in the essential oil of dill seed. L-carvone, which is also active, occurs in the essential oil of citrus and some varieties of mint.
The sprouting inhibitory activity of carvone has long been known. J.Sci.Fd Agric., vol. 20, March 1969 already describes 35 the sprouting inhibiting activity of carvone in potatoes.
Beveridge et al., Potato Res. 24 (1981), pp. 61-76, compared the sprout inhibitory effect of carvone with other So 1 ON 14 '114 [!14X s i compounds and concluded that carbone was not considered suitable for commercial purposes because of its troo low activity -s a sprouting inhibitor.
In Potato World, vol. 2. no. 4 (1985), pp. 36-38 Duncan and Boyd demonstrated the effectiveness of carbone as a sprouting inhibitor, but they also mentioned that the volatility of this agent is so high that it was not eligible for commercial use.
Other sprout inhibitors are known which satisfy the abovementioned requirements. European patent application 0 287 946 describes the sprout inhibitory effect of mint oil. This oil can be used to inhibit sprouting or to stop or interrupt any sprouting which has already developed. The advantage of the use of mint oil is that after the treatment the potatoes are directly suitable for sale without requiring that a waiting S: 15 period be observed between treatment and sale or processing.
However, it is impossible to preclude the possibility that mint oil, which has a strong taste and odor, adversely affects the sensory properties of the potato.
U.S. Patent 7,634,853 discloses the sprouting inhibitory 20 activity of monoterpenes, coming inter alia from peppermint oil and spearmint oil. These oils comprise inter alia menthol as active sprout inhibitory compound.
Surprisingly, it has now been found that an emulsion in water or in an aqueous solution of carvone alone is effective a :25 a sprouting inhibitor and/or fungoid growth inhibitor for potatoes.
Further, it has been surprisingly found that if the mixture is an emulsion in water or in an aqueous solution, a delayed release of the active compounds has been found to arise, so that 30 the active agent remains present in the space longer, the active 1 onI R \n 0 M' W I *X11 AIN -4life of the agent thereby being extended even further.
It has moreover been found, surprisingly, that an extension of the effective life of the composition in this manner can also be realized if carvone alone is present as active agent.
Accordingly, the invention also relates to a composition in the form of an emulsion in water or in an aqueous solution, with carvone alone present as active agent.
The composition according to the invention is particularly suitable for use with wa:r potatoes and industrial potatoes.
The composition according to the invention can also be used to temporarily inhibit the sprouting of seed-potatoes.
The carvone used can be D-carvone as well as L-carvone r S* a mixture of D- and L-carvones, and may be of vegetable origin or semivegetable through preparation by chemical conversion 15 from, for instance, citrus waste.
D-carvone and L-carvone exhibit an equally high activity and both may therefore be effectively used, separately as well as in a mixture.
The composition may be misted over the potatoes while they 20 are being stored in the barn or may also be contacted with the potatoes at a later stage during the storage period by misting the composition in the storage space with the support of fans in S* that space. Contact with the potatoes may also be achieved by spraying, atomizing, scattering or evaporating the composition.
25 Depending on the desired form of application, the composition may also comprise a suitable carrier, suitable solvents, fillers or other substances conventionally present.
Suitable powdery or granular carriers and fillers are starch and starch derivatives, clay, talcum and other silicas, s sand, diatomaceous earth, calcium carbonate and calcium sulfate r P I 1; IN 1 141, (gypsum) and the var'ous (co)polymers which can be used as carriers.
Suitable solvents may also be added to the composition.
For example, solvents may be of mineral origin, including aliphatic or aromatic solvents or mixtures thereof, which may or may not be chlorinated. Examples of these solvents are xylene, dichloromethane, ketones, aldehydes, alcohols such as glycerols (for instance polyethylene glycol), or derivatives or mixtures thereof. It is also possible to use solvents of animal or vegetable origin, such as linseed oil, soy bean oil or derivatives thereof. It is also possible to use mixtures of such solvents of animal, vegetable ai.d mineral origin.
A paste can be formed by adding thickeners, such as, for instance, synthetic or natural polymeric thickeners, to solutions and emulsions of the composition in the abovementioned solvents.
Suitable emulsifying agents for preparing an emulsion are cationic, anionic and non-ionic surface-active substances of animal, vegetable and mineral origin. Examples are Ca-dodecyl benzene sulfonates, nonyl phenol polygly'ol ethers, ethoxylated fatty acid alcohols or amines or derivatives or combinations thereof.
a a .4 o a) 0 a The emulsi"ier or the mixture of emulsifiers is preferably present in a ratio of about 4:1 in relation to the active 25 compound. The eventual emulsion preferably contains between 2t and 50 wt.% of active compound.
In connection with the present invention it is noted that the suitability of the various components of the formulation is partly determined by the requirements imposed on substances which come into contact with human or animal foods in general -0d I. NII R k\D IN A I 4 -6and in particular by the requirements regarding their safety for humans, animals and the environment.
S @5
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S S S 9@ S *5 St S *4 55 T 1 w The use of the composition according to the invention will be elucidated hereinafter.
First, however, the conventional storage methods for potatoes will be described.
It is conventional to store the potatoes in bulk or in large boxes in the storage space, which is mostly insulated.
By means of fans, cooler outside air can be passed through the potatoes. Optionally, the (outside) air can additionally be cooled further by means of cooling systems before being passed through the potato mass.
Storage in an o!tside pit or in a clamp silo is used for industrial potatoes nowadays, but a variant of this can also be used to store ware potatoes. This last, however, is less conventional.
15 Also, for the storage of potatoes, use can be made of cells or boxes with contents corresponding with the capacity of ventilation, heating and delivery of the product.
The bulk potatoes are first dried, stored for a few days at about 15 0 C and then cooled in about two weeks to the desired storage temperature to ensure a good injury healing of damaged potatoes. This period of injury healing is necessary to limit microbial attack and weight losses during storage.
The injury healing period of the lot takes about 14 days.
After the injury healing period, the potatoes are stored at S25 the desired storage temperature, the temperature being oee: controlled through fresh air cooling or mechanical cooling.
The desired storage temperature is 2-4 0 C for seed-potatoes, 4- 6 0 C for ware potatoes, 5-8C for French fries and dry industry, and 7-10 0 C for chips.
After a sprouting dormancy of a few months after harvest, the potato begins to exhibit an inclination to sprout (depending on variety, history and storage method). In the course of time, this inclination to sprout grows increasingly stronger.
If cooling takes place in mechanical manner (so that the desired storage temperature can be reached rapidly), the chances of early sprouting are limited already. To inhibit 1 (114 V A\I) ?19< 1' Ji' 1 1 8sprouting in optimum manner, subsequently the composition according to the present invention is used.
The use of the composition according to the invention as sprout inhibitor and as inhibitor of the development of fungi and decay bacteria is now further elucidated.
The so-called basic treatment consists of imparting the composition (in the form of, for instance, powder or granules), for instance on a conveyor which conveys the potatoes to the storage space. It is also possible to spray or atomize the composition over the potatoes (above the conveyor).
It is also possible to pass the composition to the storage space via the ventilation system. For this manner of application, the agent can for instance be atomized or sprayed in the air. For this purpose it is advantageously possible to 15 combine the mixture comprising carvone with a gaseous carrier so as to facilitate their introduction into the air stream.
The two treatments can also be combined or be performe-d one after the other.
In all cases, the composition will evaporate to a greater or lesser extent and accordingly all potatoes to be treated will come into contact with the active agent.
44 The application of the composition preferably takes place in a manner such that the concentration of carvone in the air of the storage space is between about 2 and 20 g/l air and more particularly between about 5 and 19 gg/l air. In this way the inhibitory effect on the growth of fungi and bacteria is guaranteed. At values lower than about 5 pg/1 air, the sprouting inhibition may not be guaranteed to a sufficient extent. Higher values than about 20 gg/l air may not lead to a longer sprout inhibition and therefore lead only to an unduly large use of sprout inhibiting agent.
The invention will now be further explained in and by the N following Examples.
I I Example 1 Sprout inhibiting activity Ware potatoes of the variety 'Bintje' went through an injury healing period after harvest at a temperature of and were then stored at 6 0 C. For the experiment, in each case a number of 30 potatoes (size 45-55) were treated with a sprout inhibitor having one of the compositions according to the Table below.
The sprout inhibitor was prepared by directly mixing carvone and menthol in the amounts according to the Table.
The treatment of the potatoes was effected by providin the sprout inhibitor on the bottom of a glass vessel, whereafter a rack was arranged above tne vessel, the potatoes were arranged on the rack and the vessel was closed with a 1' lid.
The potatoes were then kept at a temperature of 6°C. Twice ;a week the air in the vessel was refreshed by opening the lid of the storage space for one hour.
It was then observed after how many weeks of storage of the tubers had sprouts longer than 1 cm.
The results are shown in Table 1 below.
and 'II' in the Tables below indicate repeat- of the same tests (duplicates).
Table 1 S2S Composition Effectiveness* carvone (mg) menthol (mq) I II 112.5 12.5 27 100 25 34 34 87.5 37.5 38 62.5 62.5 >40 Number of weeks until 80% of the tubers had sprouts <onqer than 1 cm.
1, WI :04! 'SH,;A ExampQle 2 The method of Example I was repeated, with the understanding that either carvone alone or methol alone was used as sprout inhibitor. The results are shown in Table 2 below.
Composition Effectiveness* carvone menthol (mg) T 62.5 1'2 87.5 is 2 100 20 22.
112.5 21 24 -12.5 15 14 25 26 40-37 .5 30 62.5 34 34 At. 2C Number of weeks until 80% of the longer than 1 cm.
tubers had sprouts 110 4 Examnle 3 Delayed release Ware potatoes of the. variety t lBintjel were given.tm~3m pretreatment as in Example 3_ For this experiment, pr r tormulatirin a number f potatoes (size 45-55) with any sprouts removed, were ust-A.
The potatoes were assembled in an exsiccator of a volume of liters in the same manner as in Example 1 with: 1297 mg of an emulsion containing 37 wt.F6 of carvone or 11 505 l purified caraway oil (contains 95 wt.% carvone).
The composition of the emulsion is as follows: carvone* 37 wt.% Toximul" 7356 B (Stepan, 6 wt.% Soprophor K BSU (Rhine-Poulenc)** 2 wt.% water up to 100 wt.% the amount of carvone is achieved by using 39 wt.% of purified caraway oil, which contains 95 wt.% carvone.
emulsifier mixture, comprising anionic and non-ionic surface-active substances.
The amounts are such that about 480 mg carvone is present per exsiccator and hence per 20 potatoes.
The potatoes were then kept at a temperature of 6 0 C. Once a week an air sample was taken and twice a week the air in the space was refreshed by removing the lid from the exsiccator for a while.
The concentration of carvone in the air was measured.
20 The graph below (Fig. 1) plots the concentration of carvone in the air when using carvone in an emulsion and as purified caraway oil comparative test) for the duration of the experiment.
I- 12 a 60 7n o 6 C C 4Ct Fig. 1 Concentration of carvone in the air when using carvone in an emulsion and as purified caraway oil in time.potatoes will occur within a few weeks. It is therefore T-ME (DAYS 0* portant that the oncentration of carvone in the air when usingabove this carvone in an emulsion and as purified caraway oil minimum value.
It follows from the graph that the concentration of carvone when using caraway oil decreases faster than in the case where carvone is used in an emulsion. When using the emulIt is known that if the concentration of carvone falls below 5 the afteair of the storage space falls below 5 sprouting of the potatoes Swill foll occur within a few weeks It is therefore important that the concentration of carvone remain above this minimum value.
WhenIt follows from the grapin the emulsion,that the concentration of carvone when using caraway oil decreases faster than in the case where carvone is used in an emulsion. When using the emulsion, the concentration of carvone falls below 5 g/l after about 80 days. As a result, sprouting of the potatoes will follow within a few weeks.
When using carvone in the emulsion, the concentration of carvone is still higher than 10 gg/l after 90 days. Sprouting of the potatoes is thus inhibited longer.
13- Example 4 Delayed release Ware potatoes of the variety 'Bintje' were given the same pretreatment as in Examples 1 and 3.
For this experiment, per formulation a number of potatoes (size 45-55), with any sprouts removed, were used.
The following formulations were tested for their delayed release properties: A: mist formulation containing: 71 wt.% d-carv'ne 24 wt.% dl-menthol.
B: emulsion containing: 24 wt.% d-carvone 15 6 wt.% dl-menthol 6 wt.% Tensiofix hvO 2 wt.% Soprophor water to 100 C: granulate containing: •I 9 88 wt.% Tolsa sepiolite 9 wt.% d-carvone 3 wt.% dl-menthol.
The potatoes were assembled in an exsiccator of a volume of 2.7 liters in the same manner as in Example 1 v:.th: 107 41 of mist formulation A per container 333 4i of emulsion B per container 889 mg of a granulate C per container.
The potatoes were then kept at a temperature of 6 0 C. Once a week an air sample was taken and thrice a week the air in the space was refreshed by removing the lid from the exsiccator for a while.
The concentration of carvone and menthol in the air were measured.
II-~ 11 0111 k A\L) 241 NK '1I I')N 14- The graphs below (Figs. 2-4) plot the concentrat'ion of carvone and menthol in the air when using a mixture cof carvone and menthol in a mist formulation, in an emulsion and in a granulate for the duration of the experiment.
It follows from the graphs that t'-2 concentration of carvone and menthol decreases slower when these formulations are used than in the case where carvone is used as caraway (Example 3).
*0.
gi- to C 0 10 so 80 100 120 "o 160 TIME DAYS Fig. 2. Concentration of carvone and menthol in the air in time when using a mist formaulation.
100,1 70-1 06 0 100 TIME (DAYS.
Fig. 3. Concentration of carvone and menthol (U-U) in the air in time when using an emulsion.
301 ~0m/o 10-1 so. carvon 0 20 40 60 s0 Coo 1zQ' 10 160 T:ME (DAYS1 Fig. 4. Concentration of carvone and menthol (WAR) in the air in t~ie when usang a 7ranul3tp Example In this example, the synergistic activity of carvone and menthol in suppressing fungoid growth on potato tubers is demonstrated.
Potato tubers (Bintje, 45/50 mm, harvest 1993) were injured in a sterile manner. To each injury, 160 spores of the fungus Fusariu sulphureum (causing dry rot) were added. The tubers (30 pieces/con .ainer) were stored for 6 weeks at in hermetically closed plastic containers in the presence of carvone, menthol or a carvone/menthol mixture. The examination of the attack was qualitative, on the basis of the percentage of injuries exhibiting dry rot. A comparison was made with tubers that had been stored in the absence of any compound.
The rot development of these last tubers was assumed to be 100%. The results are shown in Table 3 below.
2 able 3
S
Se
I
Compound Carvone Rot Menthol Rot Carvone/ Rot applied/ dev. dev. menthol dev.
"2 rot dev.
50 83 50 100 50/200 125 73 125 100 125/125 *"23 200 43 200 100 200/50 0 250 0 250 80 check 100 This Table shows that in the presence of 200 pil carvone, still 43% of the rot development takes place, but in the presence of 250 p.1 carvone, this has been reduced to 0%.
p1 menthol does not inhibit the rot development at all.
However, the combination of 200 p1 carvone and 50 gl menthol suppresses fungoid growth completely.
sy'T 17 This test shows that menthol enhances the activity of carvone synergistically.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.
s

Claims (6)

1. A composition comprising an emulsion in water or in an aqueous solution of carvone alone as a potato sprouting and/or fungoid growth inhibitor.
2. A composition according to claim 1, which includes a carrier.
3. A composition according to claim 1 or 2 which includes a solvent and/or a filler.
4. A composition according to claim 1 and substantially as hereinbefore described with reference to the Examples.
5. Use of a composition according to any one of claims 1 to 4 to inhibit potato sprouting and/or fungal growth by contacting potatoes with said composition. 20
6. Use according to claim 5, wherein the potatoes are contacted with the composition by misting, sprayinq, atomizing, scattering or evaporating said composition. DATED this 3RD day of MARCH, 1999 25 B.V. Chemische Pharmaceutische Industrie "Luxan" DAVIES COLLISON CAVE Patent Attorneys for the Applicants Patent Attorneys for the Applicants P OPER'PTHII 10771995 DIV 15,4S.. ABSTRACT The invention relates to a composition suitable for inhibiting potato sprouting and inhibiting the growth of fungi and decay bacteria, comprising an emulsion in water or in an aqueous solution of carvone alone as the inhibitor. The invention further relates to a method for inhibiting potato sprouting by using such composition and to the use thereof. I
AU61900/98A 1993-10-04 1998-04-15 Composition suitable for inhibiting potato sprouting and/or fungoid growth Expired AU705240B2 (en)

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NL9301703 1993-10-04
NL9301703A NL9301703A (en) 1993-10-04 1993-10-04 Sprout inhibitor suitable for inhibiting the germination of potatoes.
AU10779/95A AU685201B2 (en) 1993-10-04 1994-10-03 Composition suitable for inhibiting potato sprouting and/or fungoid growth

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IL111135A (en) 2003-03-12
CA2173469C (en) 2007-06-19
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DE69427407D1 (en) 2001-07-12
ATE201808T1 (en) 2001-06-15
PE39195A1 (en) 1995-11-17
CA2173469A1 (en) 1995-04-13
EP0722272A1 (en) 1996-07-24
AU1077995A (en) 1995-05-01
US5849664A (en) 1998-12-15
DE69427407T2 (en) 2002-04-18
EP0722272B1 (en) 2001-06-06
PL180719B1 (en) 2001-03-30
PL313780A1 (en) 1996-07-22
IL111135A0 (en) 1994-12-29
ES2160691T3 (en) 2001-11-16
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WO1995009536A1 (en) 1995-04-13
AU6190098A (en) 1998-06-18

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